Organocatalyzed synthesis of fluorinated poly(aryl thioethers)

Fluorinated poly(aryl thioethers), unlike their poly(aryl ethers) counterparts, have received little attention despite excellent physical properties displayed by many polysulfides. Here the authors show a highly efficient route to fluorinated poly(aryl thioethers) via an organocatalyzed nucleophilic...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Nathaniel H. Park, Gabriel dos Passos Gomes, Mareva Fevre, Gavin O. Jones, Igor V. Alabugin, James L. Hedrick
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2017
Materias:
Q
Acceso en línea:https://doaj.org/article/0ecd61ec526244b7b2ab62ce50a86ce1
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:0ecd61ec526244b7b2ab62ce50a86ce1
record_format dspace
spelling oai:doaj.org-article:0ecd61ec526244b7b2ab62ce50a86ce12021-12-02T14:16:31ZOrganocatalyzed synthesis of fluorinated poly(aryl thioethers)10.1038/s41467-017-00186-32041-1723https://doaj.org/article/0ecd61ec526244b7b2ab62ce50a86ce12017-08-01T00:00:00Zhttps://doi.org/10.1038/s41467-017-00186-3https://doaj.org/toc/2041-1723Fluorinated poly(aryl thioethers), unlike their poly(aryl ethers) counterparts, have received little attention despite excellent physical properties displayed by many polysulfides. Here the authors show a highly efficient route to fluorinated poly(aryl thioethers) via an organocatalyzed nucleophilic aromatic substitution of silyl-protected dithiols.Nathaniel H. ParkGabriel dos Passos GomesMareva FevreGavin O. JonesIgor V. AlabuginJames L. HedrickNature PortfolioarticleScienceQENNature Communications, Vol 8, Iss 1, Pp 1-7 (2017)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Nathaniel H. Park
Gabriel dos Passos Gomes
Mareva Fevre
Gavin O. Jones
Igor V. Alabugin
James L. Hedrick
Organocatalyzed synthesis of fluorinated poly(aryl thioethers)
description Fluorinated poly(aryl thioethers), unlike their poly(aryl ethers) counterparts, have received little attention despite excellent physical properties displayed by many polysulfides. Here the authors show a highly efficient route to fluorinated poly(aryl thioethers) via an organocatalyzed nucleophilic aromatic substitution of silyl-protected dithiols.
format article
author Nathaniel H. Park
Gabriel dos Passos Gomes
Mareva Fevre
Gavin O. Jones
Igor V. Alabugin
James L. Hedrick
author_facet Nathaniel H. Park
Gabriel dos Passos Gomes
Mareva Fevre
Gavin O. Jones
Igor V. Alabugin
James L. Hedrick
author_sort Nathaniel H. Park
title Organocatalyzed synthesis of fluorinated poly(aryl thioethers)
title_short Organocatalyzed synthesis of fluorinated poly(aryl thioethers)
title_full Organocatalyzed synthesis of fluorinated poly(aryl thioethers)
title_fullStr Organocatalyzed synthesis of fluorinated poly(aryl thioethers)
title_full_unstemmed Organocatalyzed synthesis of fluorinated poly(aryl thioethers)
title_sort organocatalyzed synthesis of fluorinated poly(aryl thioethers)
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/0ecd61ec526244b7b2ab62ce50a86ce1
work_keys_str_mv AT nathanielhpark organocatalyzedsynthesisoffluorinatedpolyarylthioethers
AT gabrieldospassosgomes organocatalyzedsynthesisoffluorinatedpolyarylthioethers
AT marevafevre organocatalyzedsynthesisoffluorinatedpolyarylthioethers
AT gavinojones organocatalyzedsynthesisoffluorinatedpolyarylthioethers
AT igorvalabugin organocatalyzedsynthesisoffluorinatedpolyarylthioethers
AT jameslhedrick organocatalyzedsynthesisoffluorinatedpolyarylthioethers
_version_ 1718391648866533376